A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5919226



Internal ID22694448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12873372..12873546hg38UCSC Ensembl
chr8:12730881..12731055hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5919226
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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